quinapril

Generic: quinapril

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quinapril hydrochloride 10 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-188
Product ID 68001-188_df08337a-79bd-47c9-858a-8ee32469cfe5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077690
Listing Expiration 2026-12-31
Marketing Start 2014-02-25

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001188
Hyphenated Format 68001-188

Supplemental Identifiers

RxCUI
312748 312749 312750 314203
UNII
33067B3N2M

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name quinapril (source: ndc)
Generic Name quinapril (source: ndc)
Application Number ANDA077690 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68001-188-05)
source: ndc

Packages (1)

68001-188-05 90 TABLET in 1 BOTTLE (68001-188-05)

Ingredients (1)

quinapril hydrochloride (10 mg/1)

Linked Drug Pages (1)

Quinapril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "df08337a-79bd-47c9-858a-8ee32469cfe5", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["1b5809a8-873d-44cb-af59-e0d8fc81b385"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68001-188-05)", "package_ndc": "68001-188-05", "marketing_start_date": "20140225"}], "brand_name": "Quinapril", "product_id": "68001-188_df08337a-79bd-47c9-858a-8ee32469cfe5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68001-188", "generic_name": "Quinapril", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077690", "marketing_category": "ANDA", "marketing_start_date": "20140225", "listing_expiration_date": "20261231"}